Microglia cannibalism and efferocytosis leads to shorter lifespans of developmental microglia.


Journal

PLoS biology
ISSN: 1545-7885
Titre abrégé: PLoS Biol
Pays: United States
ID NLM: 101183755

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 14 02 2024
accepted: 29 08 2024
medline: 31 10 2024
pubmed: 30 10 2024
entrez: 30 10 2024
Statut: epublish

Résumé

The overproduction of cells and subsequent production of debris is a universal principle of neurodevelopment. Here, we show an additional feature of the developing nervous system that causes neural debris-promoted by the sacrificial nature of embryonic microglia that irreversibly become phagocytic after clearing other neural debris. Described as long-lived, microglia colonize the embryonic brain and persist into adulthood. Using transgenic zebrafish to investigate the microglia debris during brain construction, we identified that unlike other neural cell types that die in developmental stages after they have expanded, necroptosis-dependent microglial debris is prevalent when microglia are expanding in the zebrafish brain. Time-lapse imaging of microglia demonstrates that this debris is cannibalized by other microglia. To investigate features that promote microglia death and cannibalism, we used time-lapse imaging and fate-mapping strategies to track the lifespan of individual developmental microglia. These approaches revealed that instead of embryonic microglia being long-lived cells that completely digest their phagocytic debris, once most developmental microglia in zebrafish become phagocytic they eventually die, including ones that are cannibalistic. These results establish a paradox-which we tested by increasing neural debris and manipulating phagocytosis-that once most microglia in the embryo become phagocytic, they die, create debris, and then are cannibalized by other microglia, resulting in more phagocytic microglia that are destined to die.

Identifiants

pubmed: 39475879
doi: 10.1371/journal.pbio.3002819
pii: PBIOLOGY-D-24-00487
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3002819

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright: © 2024 Gordon et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

CS is a member of the PLOS Biology editorial board. The authors declare no other competing interests.

Auteurs

Hannah Gordon (H)

Department of Biological Sciences at the University of Notre Dame, Notre Dame, Indiana, United States of America.
The Center for Stem Cells and Regenerative Medicine at the University of Notre Dame, Notre Dame, Indiana, United States of America.

Zachary T Schafer (ZT)

Department of Biological Sciences at the University of Notre Dame, Notre Dame, Indiana, United States of America.

Cody J Smith (CJ)

Department of Biological Sciences at the University of Notre Dame, Notre Dame, Indiana, United States of America.
The Center for Stem Cells and Regenerative Medicine at the University of Notre Dame, Notre Dame, Indiana, United States of America.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH